Ferroptosis-IN-21
Based on 1 Customer Validation
Ferroptosis-IN-21 is a ferroptosis inhibitor that protects against renal I/R injury by suppressing ferroptosis and directly scavenging peroxyl radicals. Ferroptosis-IN-21 displays broad-spectrum anti-ferroptotic efficacy across multiple inducers in renal tubular epithelial cells, with nanomolar potency and robust suppression of lipid Reactive Oxygen Species (ROS). Ferroptosis-IN-21 significantly ameliorates renal I/R injury in mice, reducing histological damage, functional impairment, and inflammatory cytokine expression, while decreasing lipid peroxidation biomarkers such as 4-hydroxynonenal. Ferroptosis-IN-12 can be used for research in the field of ferroptosis-targeted drug development.
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- Pureté : 99.88%
- CAS No.: 6640-50-2
- Formule: C9H11NO
- Masse moléculaire:149.19
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Stockage:
RT, protect from light.
In solvent -80°C, 1 year , -20°C, 6 months
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Activité biologique
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Chemical Information
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Solvant et solubilité
- Pureté et documentation
- Références
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Help & FAQs
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HY-W000806
ThallineTetrahydroquinoline Derivative -
HY-107870
1,2,4-Triazole-3-carboxylic acid, 97%Biochemical Assay Reagent -
HY-W250457
Ondansetron impurity 6Drug Impurity -
HY-W338780
Cyclohexane-1,2,3,4,5,6-hexacarboxylic acidMetal-organic Framework -
HY-W250457R
9-Methyl-3-methylene-2,3-dihydro-1H-carbazol-4(9H)-one (Standard) -
HY-W040960R
H-1,2,4-Triazole-3-carboxamide (Standard)
Activité biologique
Description
In Vitro
Ferroptosis-IN-21 (compound 6) (0.01-10 μM, 24 h) exhibits nanomolar cytoprotective activity (EC50 = 61.7 nM) and completely reverses cell death at 200 nM in HT-1080 cells, and dose-dependently protects Human Kidney Cortex epithelial cells (HKC) and Human Kidney 2 (HK-2) cells from ferroptosis induced by RSL-3 (HY-100218A) and FIN-56, confirming its broad-spectrum efficacy[1].
Ferroptosis-IN-21 (50-500 nM, 24 h) significantly suppresses RSL-3-induced lipid ROS accumulation and MDA elevation, and has no effect on GPX4 protein levels[1].
Ferroptosis-IN-21 (10 µM) does not chelate iron ions, ruling out an iron-chelating mechanism[1].
Ferroptosis-IN-21 (1-80 µM, 30 min) exhibits potent direct radical scavenging activity in Cell-free DPPH assay[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HT-1080, HKC and HK-2 cells
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Concentration:0.01-10 μM
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Incubation Time:24 h
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Result:Exhibited nanomolar cytoprotective activity with an EC50 of 61.7 nM in HT-1080 cells.
Completely reversed RSL3-induced cell death in HT-1080 cells at the dose of 200 nM.
Exhibited significant cytoprotective effects on both HKC and HK-2 cells under RSL3-induced ferroptosis, displaying a concentration-dependent relationship, with the EC50 values of 361 and 258 nM, respectively.
Effectively inhibited FIN56-induced cell death in both HKC and HK-2 cells.
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Cell Line:HKC cells
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Concentration:500 nM
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Incubation Time:24 h
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Result:Did not significantly alter GPX4 protein expression in either untreated or RSL3- stimulated cells.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Male C57BL/6 mice (8-12 weeks old) subjected to bilateral renal ischemia (40 min) and reperfusion (24 h) [1]
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Dosage:5 and 10 mg/kg
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Administration:i.p., 24 hours and 1 hour pre-treatment
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Result:Reduced the serum creatinine, blood urea nitrogen (BUN), and kidney coefficient relative to the I/R group.
Conferred substantial structural protection, with the 10 mg/kg dose yielding the most notable histological preservation.
Markedly suppressed mRNA expression levels of KIM-1 and NGAL in a dose-dependent manner.
Significantly reduced the expression of TNF-α, IL1-β, IL-6, and MCP-1 upregulated by I/R insult in a dose-dependent manner, indicating an anti-inflammatory effect.
Markedly reduced I/R-induced 4-HNE accumulation.
Chemical Information
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CAS No. 6640-50-2
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Appearance Solid
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Masse moléculaire 149.19
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Formule C9H11NO
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Color Off-white to yellow
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SMILES
OC1=CC=CC2=C1NCCC2
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Synonyms
1,2,3,4-Tetrahydroquinolin-8-ol; 8-hydroxy-1,2,3,4-tetrahydroquinoline
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
RT, protect from light
In solvent -80°C 1 year -20°C 6 months
Solvant et solubilité
In Vitro:
DMSO : ≥ 100 mg/mL (670.29 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
In Vivo:
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 5 mg/mL (33.51 mM); Clear solution
This protocol yields a clear solution of ≥ 5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (50.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 5 mg/mL (33.51 mM); Clear solution
This protocol yields a clear solution of ≥ 5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (50.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Pureté et documentation
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Fiche technique (283 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Instruction de manipulation (2659 KB)
Références
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
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| DMSO | 1 mM | 6.7029 mL | 33.5143 mL | 67.0286 mL | 167.5716 mL |
| 5 mM | 1.3406 mL | 6.7029 mL | 13.4057 mL | 33.5143 mL | |
| 10 mM | 0.6703 mL | 3.3514 mL | 6.7029 mL | 16.7572 mL | |
| 15 mM | 0.4469 mL | 2.2343 mL | 4.4686 mL | 11.1714 mL | |
| 20 mM | 0.3351 mL | 1.6757 mL | 3.3514 mL | 8.3786 mL | |
| 25 mM | 0.2681 mL | 1.3406 mL | 2.6811 mL | 6.7029 mL | |
| 30 mM | 0.2234 mL | 1.1171 mL | 2.2343 mL | 5.5857 mL | |
| 40 mM | 0.1676 mL | 0.8379 mL | 1.6757 mL | 4.1893 mL | |
| 50 mM | 0.1341 mL | 0.6703 mL | 1.3406 mL | 3.3514 mL | |
| 60 mM | 0.1117 mL | 0.5586 mL | 1.1171 mL | 2.7929 mL | |
| 80 mM | 0.0838 mL | 0.4189 mL | 0.8379 mL | 2.0946 mL | |
| 100 mM | 0.0670 mL | 0.3351 mL | 0.6703 mL | 1.6757 mL |
Ferroptosis-IN-21 Related Classifications
HY-W002942 Related Classifications
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Keywords
- Ferroptosis-IN-21
- 6640-50-2
- 1,2,3,4-Tetrahydroquinolin-8-ol
- 8-hydroxy-1,2,3,4-tetrahydroquinoline
- Free Radical Scavengers
- Ferroptosis
- Reactive Oxygen Species (ROS)
- ferroptosis
- AKT
- renal I/R injury
- peroxyl radicals
- anti-ferroptotic
- renal tubular epithelial cells
- ROS
- histological damage
- inflammatory cytokine expression
- lipid peroxidation biomarkers
- renal ischemia-reperfusion mice model
- HT-1080
- HKC
- HK-2
- Inhibitor
- inhibitor
- inhibit